LDH info

Canonical Allele Identifier: CA64315371
Gene: PARD3B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1207421

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.205285870A>G , CM000664.2:g.205285870A>G GRCh38
NC_000002.11:g.206150594A>G , CM000664.1:g.206150594A>G GRCh37
NC_000002.10:g.205858839A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001302769.1:c.2186-14660A>G VV NP_001289698.1:p.=
NM_057177.6:c.2186-15594A>G VV NP_476518.4:p.=
NM_152526.5:c.2000-14660A>G VV NP_689739.4:p.=
NM_205863.3:c.2186-14660A>G VV NP_995585.2:p.=
XM_011510550.1:c.2186-14660A>G XP_011508852.1:p.=
XM_011510551.1:c.2186-14660A>G XP_011508853.1:p.=
XM_011510552.1:c.2210-14660A>G XP_011508854.1:p.=
XM_011510553.1:c.2210-14660A>G XP_011508855.1:p.=
XM_011510552.2:c.2210-14660A>G XP_011508854.1:p.=
XM_011510553.2:c.2210-14660A>G XP_011508855.1:p.=
XM_017003283.1:c.2150-14660A>G XP_016858772.1:p.=
XM_017003284.1:c.2120-14660A>G XP_016858773.1:p.=
XM_017003285.1:c.2024-14660A>G XP_016858774.1:p.=
XM_017003286.1:c.2018-14660A>G XP_016858775.1:p.=
XM_017003287.1:c.2210-14660A>G XP_016858776.1:p.=
XM_017003288.1:c.2210-14660A>G XP_016858777.1:p.=
XM_017003289.1:c.1685-14660A>G XP_016858778.1:p.=
XM_017003290.1:c.1589-14660A>G XP_016858779.1:p.=
XM_017003291.1:c.1589-14660A>G XP_016858780.1:p.=
XM_017003292.1:c.1589-14660A>G XP_016858781.1:p.=
XM_017003293.1:c.1589-14660A>G XP_016858782.1:p.=
NM_001302769.2:c.2186-14660A>G VV MANE Preferred NP_001289698.1:p.=
ENST00000349953.7:n.2186-14660A>G ENSP00000340280.3:p.=
ENST00000351153.5:n.2186-15594A>G ENSP00000317261.2:p.=
ENST00000358768.6:n.2000-14660A>G ENSP00000351618.2:p.=
ENST00000406610.6:c.2186-14660A>G ENSP00000385848.2:p.=
ENST00000462231.5:c.2186-14660A>G ENSP00000473503.1:p.=
ENST00000613457.4:n.1778-14660A>G ENSP00000484434.1:p.=
ENST00000614500.3:n.1964-15594A>G ENSP00000481918.1:p.=
ENST00000622699.2:n.1964-14660A>G ENSP00000482649.1:p.=